Towards improved animal models of neonatal white matter injury associated with cerebral palsy

被引:95
作者
Silbereis, John C. [3 ,4 ,5 ]
Huang, Eric J. [6 ]
Back, Stephen A. [1 ,2 ]
Rowitch, David H. [3 ,4 ,5 ,7 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Pediat, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97239 USA
[3] Univ Calif San Francisco, Eli & Edythe Broad Inst Stem Cell Res & Regenerat, Dept Pediat, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Eli & Edythe Broad Inst Stem Cell Res & Regenerat, Dept Neurosurg, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[6] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[7] Univ Calif San Francisco, Div Neonatol, San Francisco, CA 94143 USA
关键词
OLIGODENDROCYTE LINEAGE MATURATION; PERINATAL SUBVENTRICULAR ZONE; OXIDE SYNTHASE EXPRESSION; CENTRAL-NERVOUS-SYSTEM; ISCHEMIC BRAIN-DAMAGE; DEVELOPING RAT-BRAIN; HYPOXIA-ISCHEMIA; PERIVENTRICULAR LEUKOMALACIA; PRETERM INFANTS; MULTIPLE-SCLEROSIS;
D O I
10.1242/dmm.002915
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Newborn neurological injuries are the leading cause of intellectual and motor disabilities that are associated with cerebral palsy. Cerebral white matter injury is a common feature in hypoxic-ischemic encephalopathy (HIE), which affects fullterm infants, and in periventricular leukomalacia (PVL), which affects preterm infants. This article discusses recent efforts to model neonatal white matter injury using mammalian systems. We emphasize that a comprehensive understanding of oligodendrocyte development and physiology is crucial for obtaining new insights into the pathobiology of HIE and PVL as well as for the generation of more sophisticated and faithful animal models.
引用
收藏
页码:678 / 688
页数:11
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